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Research 751–780 of 1000+
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Solidariedade e plasticidade fenotípica entre indivíduos de Thunbergia grandiflora Roxb. e Russelia equisetiformis Schltdl. & Cham.
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Ivarmacitinib in atopic dermatitis presenting with prurigo nodularis-like lesions and alopecia areata: a case report
- Systemic testosterone induces structural, immunological, and sex steroid receptor changes in human XX skin
- Impaired turnover of autophagolysosomes in cathepsin L deficiency
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Testosterone enantate
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Clonal expansion from standing genetic variation underpins the evolution of an emerging plant pathogen in Australia
- Molecular basis of androgen insensitivity
- Morpho-Regulation of Ectodermal Organs
- Cell Polarization Defects in Early Heart Development
- Pre‐polycystic ovary syndrome and polymenorrhoea as new facets of polycystic ovary syndrome (PCOS): Evidences from a single centre data set
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Impact of Testosterone on Hair and Skin
- Functional analysis of thymosin beta-4 using over-expressing transgenic mice
- In This Issue
- The Role of Genes and Skin Microbiome in the Development of Seborrheic Dermatitis
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Histocultures and Their Use
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report